Canonical Allele Identifier: CA349846967
Gene: COL3A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.189873789A>C (hg19) chr2:g.189009063A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189009063A>C , CM000664.2:g.189009063A>C GRCh38
NC_000002.11:g.189873789A>C , CM000664.1:g.189873789A>C GRCh37
NC_000002.10:g.189582034A>C NCBI36
NG_007404.1:g.39691A>C , LRG_3:g.39691A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000450867.2:c.3566A>C ENSP00000415346.2:p.Asp1189Ala
ENST00000304636.9:c.3665A>C MANE Select ENSP00000304408.4:p.Asp1222Ala
ENST00000304636.7:c.3665A>C ENSP00000304408.3:p.Asp1222Ala
ENST00000317840.9:c.2756A>C ENSP00000315243.6:p.Asp919Ala
ENST00000487010.1:n.762A>C
NM_000090.3:c.3665A>C , LRG_3t1:c.3665A>C NP_000081.1:p.Asp1222Ala
NM_000090.4:c.3665A>C MANE Select NP_000081.2:p.Asp1222Ala
Search 100 bp 5'
Search 100 bp 3'